APEC Regulatory Harmonization Steering Committee (RHSC)
Results
Working group
The working group’s mandate was to deliver on Key Terms and Definitions for Machine Learning-enabled Medical Devices.
Working group
Harmonize the regulatory requirements for medical devices that are intended for a particular individual, considering unique characteristics and risks associated with each type of device.
Working group
A working group on Clinical evidence for in vitro diagnostic (IVD) medical devices
Working group
Review and update the GHTF/SG1/N045:2008 Principles of In Vitro Diagnostic (IVD) Medical Devices Classification.
Working group
A working group for Clinical Evidence for IVD Medical Devices
Working group
Manage cybersecurity risks in medical devices through a life-cycle approach. Striking the right balance between pre-market and post-market requirements.
Working group
Registries of patients undergoing medical device procedures represent a growing potential electronic resource for local and global medical device evaluation and tracking.
Working group
Improve the effectiveness and efficiency of the pre-market review process by promoting increased global harmonization.
Working group
Develop good review practices for pre-market reviews and evaluations.
Working group
Ensure alignment of IMDRF QMS and risk management documents with current international standards